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FDA 510(k)

PEDIATRIC INTUBATION CIRCUIT

K-Number: K840056 · 1984-02-10

ApplicantAckrad Laboratories
Decision Date1984-02-10
Product CodeCAI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PEDIATRIC INTUBATION CIRCUIT is the device name listed in this FDA 510(k) record. The listed applicant is Ackrad Laboratories. It received FDA 510(k) clearance on 1984-02-10 under 510(k) number K840056. The device is classified under product code CAI. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PEDIATRIC INTUBATION CIRCUIT?

PEDIATRIC INTUBATION CIRCUIT is a medical device that received FDA 510(k) clearance on 1984-02-10. The listed applicant is Ackrad Laboratories. The 510(k) number is K840056.

When did PEDIATRIC INTUBATION CIRCUIT receive FDA 510(k) clearance?

PEDIATRIC INTUBATION CIRCUIT received FDA 510(k) clearance on 1984-02-10, under 510(k) number K840056.

Who is the listed applicant for PEDIATRIC INTUBATION CIRCUIT?

The FDA 510(k) record lists Ackrad Laboratories as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PEDIATRIC INTUBATION CIRCUIT?

The FDA product code for PEDIATRIC INTUBATION CIRCUIT is CAI.

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Other records listing Ackrad Laboratories as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K021272SIB CATHETER, MODEL 61-7005K020954H/S PROCEDURE TRAY (5F), H/S PROCEDURE TRAY (7F), H/S ELLIPTOSPHERE PROCEDURE TRAY & MULTIPURPOSE PROCEDURE TRAYK020951H/S CATHETER SET (5F), MODEL 61-5005; H/S CATHETER SET (7F), MODEL 61-5007K970492INTRAUTERINE INSEMINATION AND SONOHYSTEROGRAPHY CATHETERK961752H/S CATHETER SET(61-3005, 61-3007, 61-3605, 61-3607)K940176ACKRAD IUI SET FOR INTRAUTERINE INSEMINATION

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Related Devices (Code: CAI)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K954480CONDENSATE COLLECTION KITNova-VentrxK953787UNICOR, INC. ADULT ANESTHESIA BREATHING CIRCUITUnicor, Inc.K953788UNICOR, INC. GAS SAMPLING LINES & CONNECTORSUnicor, Inc.K952016PRIMA PEDIATRIC GAS SAMPLING CIRCUITSPrima, Inc.K952018PRIMA COAXIAL CIRCUITSPrima, Inc.K952020PRIMA PEDIATRIC ANESTHESIA CIRCUITSPrima, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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